Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophy. [electronic resource]
Producer: 20150311Description: 299-310 p. digitalISSN:- 1939-327X
- 1-Acylglycerol-3-Phosphate O-Acyltransferase -- metabolism
- 3T3-L1 Cells
- Adipocytes, White -- physiology
- Adolescent
- Adult
- Amino Acid Sequence
- Animals
- Base Sequence
- Carrier Proteins -- genetics
- Diabetes Mellitus, Type 2 -- genetics
- Family Health
- Female
- Frameshift Mutation
- Humans
- Hyperlipoproteinemia Type IV -- genetics
- Insulin Resistance -- genetics
- Lipodystrophy, Familial Partial -- genetics
- Male
- Mice
- Middle Aged
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Pedigree
- Perilipin-1
- Phosphoproteins -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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